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Erin K. Kennedy · SciRah

Researcher profile · Semantic Scholar

Erin K. Kennedy

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Erin K. Kennedy — researcher profile on SciRah

h-index: 5
Works: 7
Citations: 321

Most-cited papers

Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD).
P. Chakraborty, K. Schmitz-Abe, Erin K. Kennedy, Hapsatou Mamady +31 more
2014Blood184 citations Open access
Semantic Scholar
A Wee1 checkpoint inhibits anaphase onset
Noel Lianga, Elizabeth C. Williams, Erin K. Kennedy, Carole Doré +4 more
2013Journal of Cell Biology79 citations Open access
Semantic Scholar
The Neurospora crassa TOB Complex: Analysis of the Topology and Function of Tob38 and Tob37
Sebastian W. K. Lackey, Jeremy G. Wideman, Erin K. Kennedy, N. E. Go +1 more
2011PLoS ONE23 citations Open access
Semantic Scholar
Cdk1 phosphorylation of Esp1/Separase functions with PP2A and Slk19 to regulate pericentric Cohesin and anaphase onset
Noel Lianga, Carole Doré, Erin K. Kennedy, E. Yeh +5 more
2018PLoS Genetics18 citations Open access
Semantic Scholar
Redundant Regulation of Cdk1 Tyrosine Dephosphorylation in Saccharomyces cerevisiae
Erin K. Kennedy, Michael Dysart, Noel Lianga, Elizabeth C. Williams +4 more
2015Genetics15 citations Open access
Semantic Scholar
A Wee 1 checkpoint inhibits anaphase onset
Noel Lianga, Elizabeth C. Williams, Erin K. Kennedy, Carole Doré +4 more
20132 citations
Semantic Scholar
A Wee 1 checkpoint inhibits anaphase onset
Noel Lianga, Elizabeth C. Williams, Erin K. Kennedy, Carole Doré +4 more
20130 citations
Semantic Scholar

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Adam D. Rudner — researcher profile on SciRah
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